FeaturedNewsTrending Stocks

Acurx Pharmaceuticals Stock Is Higher By 42% In June…Here’s Why The Bears Are Staying Away ($ACXP)

Markets have been terrible. In fact, few stocks have weathered the bearish storm as all major indexes break below bear market territory. However, not all stocks are in decline. Acurx Pharmaceuticals (NASDAQ: ACXP) indeed isn’t. Its shares are higher by more than 42% since the start of the month.

Moreover, it’s showing that it has the firepower to decouple not only from broader market weakness but also from biotech sector declines. So, why is the investor interest in $ACXP sending its share price higher? Well, put most simply, they continue to do everything right to get a CDI treatment drug candidate to market that has best-in-class front-line treatment potential. 

While that’s excellent news for ACXP and its investors from an ongoing Phase2 clinical perspective, the more driving part of the ACXP equation is that its ibezapolstat candidate demonstrates things others can’t. And that difference could be attracting the interest of several big pharma companies wanting exposure to an estimated $1.6 billion CDI treatment market. But, one may ask, doesn’t big pharma have its own candidates in the CDI pipeline? The answer is Yes. However, their data is unimpressive. 

A Gem Getting Uncovered

In fact, it’s more than unimpressive; several companies have missed primary endpoints and are re-evaluating their candidate altogether. Some may even drop out or dramatically shift clinical focus on endpoint intent. But, while they are scrambling, Acurx Pharmaceuticals looks most promising in its mission, with data supporting its drug candidate as the last company standing in a race to capture the lion’s share of the estimated $1.6 billion CDI treatment market opportunity. 

What happened to the competition? Well, over the past decade, disappointing clinical results have led to several big pharma companies dropping off the clinical radar. Those still pursuing its CDI treatment candidate may be doing so with hopes of potentially treating, at best, niche indications of the infection. The latest disappointing data came from Pfizer (NYSE: PFE), which missed meeting its primary endpoints in its Phase 3 CLOVER trial to treat C. diff. But they aren’t the only ones licking their wounds. 

Sanofi (NYSE: SNY) missed its endpoints back in 2017, and more recently, Summit Therapeutics (NYSE: SMMT) published topline results that were far from impressive. In fact, that miss resulted in them trying to change the primary endpoints in its Phase 3 trial, something the FDA didn’t accommodate. Those three weren’t the only ones disappointed to date. 

Another pharmaceutical company, Finch Therapeutics (NASDAQ: FNCH), saw a setback when it received a clinical hold letter from the FDA about concerns over its SARS-CoV-2 donor screening protocols. While Finch announced that the FDA hold was lifted and enrollment would resume in 2H 2022, they still lost considerable clinical momentum. It’s appropriate to note that FNCH’s Phase 2 data was impressive compared to Pfizer, Sanofi, and Summit. It showed that 80.3% of trial participants receiving a single administration of its candidate following standard-of-care antibiotics achieved sustained clinical cure through eight weeks. Promising, yes. Better than ACXP? No. 

Best-In-Class Data For ACXP’s Ibezapolstat

Acurx’s candidate published Phase 2a data that appears to be significantly better. The most significant advantage could be that compared to Finch’s candidate, which focuses on the microbiome as a single dimension and has shown only a reduction in recurrent infection, ACXP’s ibezapolstat is a dual impact drug that addresses the direct infection and, to date, avoids recurrent infection altogether. Not only that, it restores the microbiome, a critical consideration. 

That difference alone endorses a persuasive and data-justified argument that ACXP’s candidate is seemingly better than Finch’s one-dimension drug in cases of multiple recurrent infections. If that’s the case, ACXP’s candidate checks additional boxes to become the preferred first-line treatment. And other than Finchs’, no other candidate looks close to emerging as a serious threat to ACXP’s ibezapolstat’s intended front-line position. 

That’s potentially excellent news for ACXP. And it’s why ACXP could already be on Big Pharma’s shortlist for acquisition or licensing terms to earn the lion’s share of a lucrative market opportunity. 

Is Big Pharma Looking For A Connection?

Speculation is that Pfizer could be the first to call. During its CLOVER trial update commentary, investors were zeroed in on Pfizer expressing their interest in pursuing the over one billion dollar market opportunity. Still, interest and ability are two different clinical beings, and in the drug industry, only the latter matters. 

With that said, don’t think PFE is blinded by unwarranted optimism. They know its candidate failed to meet endpoints. Moreover, they likely know, at best, its candidate, if approved, would be relegated to treating fringe and niche CDI treatment indications. Therefore, spending up to hundreds of millions of dollars more to advance an unpromising drug candidate makes little to no sense. 

What does make sense is for deep-pocketed Pfizer to cozy up with the presumed CDI treatment drug frontrunner. In this case, with data supporting the presumption, Acurx is the likely recipient of their first call. Remember that PFE doesn’t invest billions to earn a backstage pass. Instead, history indicates that what they can’t produce, they acquire. And with ACXP showing evidentiary promise as one of the only companies left to bring an effective and comprehensive CDI treatment to market, it may be wise to consider a fair price for its lead asset. 

Better news for ACXP and investors is that the price point could be hefty, with ACXP bargaining from a position of strength. Remember, data supports the potential for ibezapolstat to become the front-line therapy to treat over 500,000 patients who get CDI each year. Of those 500,000, more than 20,000 patients per year die. So, while the term infection is used, don’t underestimate its potential 4% outcome. CDI can be fatal.

A much-Needed Cure For CDI

It’s why the race to find a treatment, better yet, a cure for CDI, is a persistent pursuit. And that’s exactly what ACXP may be serving up. So don’t think Pfizer calling on Acurx is overly speculative. They would be dialing because ACXP’s Phase2a data showed 100% cure after 10 days of treatment and 100% sustained cure after a 30-day follow-up. Thus, the totality of data, even noting Finch’s one-dimensional eight-week sustained cure, shows ACXP’s Phase 2a data to date constitutes the best clinical data seen in the CDI space. 

Also strengthening its likelihood of earning front-line status, ACXP’s CDI candidate demonstrates restoration of the patient’s microbiome during treatment, which is highly unusual for an antibiotic. Considering that, it’s reasonable to consider ibezapolstat as a potential “dual impact” therapy because it restores the microbiome while tending to the acute infection. 

More in ACXP’s favor and likely attracting industry attention is that the data from its Ph2a trial was so impressive that it led the Trial Oversight Committee and the Scientific Advisory Board to allow for early termination of its Phase 2a trial and advance straight into a Phase 2b study. Furthermore, that jump was allowed after data on just ten patients showed a 100% cure rate and 100% sustained cure after follow-up. 

They save time and resources from that allowance. They benefit further from the FDA already granting ACXP a Qualified Infectious Disease Product (QIDP) and a fast-track designation for the company’s ibezapolstat treatment. Interest in their help getting a better drug to market faster could stem from knowing that Vancomycin, the current standard of care for CDI, has a recurrent infection rate of up to 40%, meaning it is not as effective in long-term treatment.

The Market Is Validated

Also, remember that an approved ibezapolstat will likely meet overwhelming demand. A 2017 update of the Clinical Practice Guidelines for C. difficile infection by the Infectious Diseases Society of America (IDSA) and Society or Healthcare Epidemiology of America (SHEA) indicates that C. difficile infection presents a significant problem to those in healthcare settings and among the general population. The disease is so prevalent in hospitals and long-term care facilities that the New England Journal of Medicine called C. difficile one of the most common causes of health-care-associated infections in hospitals.

While there is already a plethora of company-published data to support and attract interest, there’s more to consider. And it’s again favorable to ACXP. Data published from ACXP’s Phase 2a trial in Clinical Infectious Diseases, one of the most respected journals in the medical community, indicates that ibezapolstat is well positioned to earn the front-line treatment crown. According to the article, ibezapolstat showed ideal traits as an oral antibiotics candidate, demonstrating a highly potent response against C. difficile, good tolerability, and limited gastrointestinal absorption. That resulted in very high fecal concentrations, which may reach three orders of magnitude above the MIC for C. difficile.

The article further noted that in addition to the ibezapolstat treatment being highly effective at killing C. difficile, it appears to do so while maintaining the populations of helpful bacteria in the gut microbiome. These signs indicate that the treatment may do more than cure CDI in the short term; it can significantly reduce the likelihood of recurrent infection. 

Will Suitors Want To Play?

What’s it all mean? Put simply, ACXP could be in play. Moreover, things could move quickly, noting that the cost to partner with a Phase 2 company over a Phase 3 company can amount to hundreds of millions of dollars. Yes, hundreds of millions. Just look at before and after market cap shots of companies making that leap. It’s a valid indication of how valuable being a Phase 3 trial with compelling, best-in-class data can be. 

The bottom line… Acurx is in the right place with the most promising CDI treatment drug to make a deal. And while several companies may be interested near-term to partner or license, the chatter centers around Pfizer being the ideal and most likely suitor. 

If so, whether in Phase 2 or Phase 3, ACXP investors could be in for an exciting ride in 2022. Catching that action from the inside and looking out may be the better place to reside. After all, what may be considered chump change from Pfizer, or another pharma player, would be a windfall for Acurx Pharmaceuticals and its investors. And the way things could play out, both may get that benefit. 

 

Disclaimers: Hawk Point Media, Group, Llc, (HPM) and its wholly-owned asset, Level3Trading is responsible for the production and distribution of this content. Level3Trading is not operated by a licensed broker, a dealer, or a registered investment adviser. It should be expressly understood that under no circumstances does any information published herein represent a recommendation to buy or sell a security. Our reports/releases are a commercial advertisement and are for general information purposes ONLY. We are engaged in the business of marketing and advertising companies for monetary compensation. Never invest in any stock featured on our site or emails unless you can afford to lose your entire investment. The information made available by Level3Trading is not intended to be, nor does it constitute, investment advice or recommendations. The contributors may buy and sell securities before and after any particular article, report and publication. In no event shall Level3Trading be liable to any member, guest or third party for any damages of any kind arising out of the use of any content or other material published or made available by Level3Trading, including, without limitation, any investment losses, lost profits, lost opportunity, special, incidental, indirect, consequential or punitive damages. Past performance is a poor indicator of future performance. The information in this video, article, and in its related newsletters, is not intended to be, nor does it constitute, investment advice or recommendations. Level3Trading strongly urges you conduct a complete and independent investigation of the respective companies and consideration of all pertinent risks. Readers are advised to review SEC periodic reports: Forms 10-Q, 10K, Form 8-K, insider reports, Forms 3, 4, 5 Schedule 13D. For some content, Level3Trading, its authors, contributors, or its agents, may be compensated for preparing research, video graphics, and editorial content. As part of that content, readers, subscribers, and website viewers, are expected to read the full disclaimers and financial disclosures statement that can be found Level3trading.com/disclaimers. HPM has been compensated up to three-thousand -five-hundred-dollars by a third party to produce and syndicate content for the company featured above. Contributors reserve the right, but are not obligated to, submit articles for fact-checking prior to publication. Contributors are under no obligation to accept revisions when not factually supported. Furthermore, because contributors are compensated, readers and viewers of this content should always assume that content provided shows only the positive side of companies, and rarely, if ever, highlights the risks associated with investment. Thus, readers and viewers should accept the content as an advertorial that highlights only the best features of a company. Never take opinion, articles presented, or content provided as a sole reason to invest in any featured company. Investors must always perform their own due diligence prior to investing in any publicly traded company and understand the risks involved, including losing their entire investment.

The Private Securities Litigation Reform Act of 1995 provides investors a safe harbor in regard to forward-looking statements. Any statements that express or involve discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, goals, assumptions or future events or performance are not statements of historical fact may be forward looking statements. Forward looking statements are based on expectations, estimates, and projections at the time the statements are made that involve a number of risks and uncertainties which could cause actual results or events to differ materially from those presently anticipated. Forward looking statements in this action may be identified through use of words such as projects, foresee, expects, will, anticipates, estimates, believes, understands, or that by statements indicating certain actions & quote; may, could, or might occur. Understand there is no guarantee past performance will be indicative of future results. Investing in micro-cap and growth securities is highly speculative and carries an extremely high degree of risk. It is possible that an investors investment may be lost or impaired due to the speculative nature of the companies profiled.

Related Articles

Leave a Reply

Your email address will not be published. Required fields are marked *

Back to top button